On-Site Clinical Research Coordinator - 24 hrs/week

IQVIA; Novi (MI); On-site; USD 48,000 - 58,000; Full time

Job summary

IQVIA is hiring a Clinical Research Coordinator to support studies under the supervision of a principal investigator. On-site duties include hands-on procedures, community outreach, and ensuring patient safety and protocol compliance.

The role requires 1+ years in clinical research, knowledge of GCP, and strong data collection skills. This position is not sponsorship eligible and offers a base pay range with potential incentives.

Qualifications

• Bachelor’s degree preferred or equivalent combination of education and relevant experience.
• Minimum 1+ years of relevant work experience in clinical research.
• Working knowledge of clinical trials, GCP principles, and medical terminology.
• Experience with prescreening patients based on inclusionary/exclusionary criteria.
• Familiarity with patient chart/medical record review.
• Ability to support patient study visits.
• Strong attention to detail and ability to establish effective working relationships.
• Proficiency with EDC systems, data entry accuracy, and query management.

Responsibilities

• Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
• Coordinate clinical research studies and maintain compliance with protocols and GCP guidelines.
• Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
• Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.
• Collect and accurately record clinical data in case report forms (CRFs).
• Collaborate with investigators and monitors, addressing queries and ensuring data quality.
• Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.

Skills

Clinical research knowledge

Attention to detail

Communication

Patient safety and ethics

Education

Bachelor’s degree or equivalent

Tools

EDC systems

Data entry accuracy

Query management

Job description

IQVIA is hiring a Clinical Research Coordinator to support studies under the supervision of a principal investigator. On-site duties include hands-on procedures, community outreach, and ensuring patient safety and protocol compliance.

The role requires 1+ years in clinical research, knowledge of GCP, and strong data collection skills. This position is not sponsorship eligible and offers a base pay range with potential incentives.